Expression Levels of an Alpha-Synuclein Transcript in Blood May Distinguish between Early Dementia with Lewy Bodies and Parkinson's Disease.
Laura Marsal-GarcíaAintzane UrbizuLaura ArnaldoJaume CampdelacreuDolores VilasLourdes IspiertoJordi Gascón-BayarriRamón ReñéRamiro ÁlvarezKatrin BeyerPublished in: International journal of molecular sciences (2021)
Lewy body diseases (LBD) including dementia with Lewy bodies (DLB) and Parkinson disease (PD) are characterized by alpha-synuclein pathology. DLB is difficult to diagnose and peripheral biomarkers are urgently needed. Therefore, we analyzed the expression of five alpha-synuclein gene (SNCA) transcripts, SNCAtv1, SNCAtv2, SNCAtv3, SNCA126, and SNCA112, in 45 LBD and control temporal cortex samples and in the blood of 72 DLB, 59 PD, and 54 control subjects. The results revealed overexpression of SNCAtv1 and SNCA112 in DLB, and SNCAtv2 in PD temporal cortices. In DLB blood, diminution of all SNCA transcripts was observed. SNCAtv1 and SNCAtv2 were diminished in PD with disease onset before 70 years. SNCAtv3, driven by its own promoter, showed opposite expression in early DLB and PD, suggesting that its amount may be an early, DLB specific biomarker. Correlation between blood transcript levels and disease duration was positive in DLB and negative in PD, possibly reflecting differences in brain alpha-synuclein aggregation rates associated with differences in disease courses. In conclusion, SNCA transcripts showed a disease-specific increase in the brain and were diminished in blood of LBD patients. SNCAtv3 expression was decreased in early DLB and increased in early PD and could be a biomarker for early DLB diagnosis.
Keyphrases
- parkinson disease
- poor prognosis
- deep brain stimulation
- end stage renal disease
- resting state
- functional connectivity
- cell proliferation
- binding protein
- mild cognitive impairment
- gene expression
- chronic kidney disease
- dna methylation
- rna seq
- single cell
- patient reported outcomes
- newly diagnosed
- prognostic factors
- peritoneal dialysis
- multiple sclerosis
- genome wide